What is NDC 63629-1783?

63629-1783 is the product NDC for Cimetidine, Cimetidine 300 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 63629. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Cimetidine?

21 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cimetidine NDC 63629-1783 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63629-1783Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63629-1783Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
63629-1783-1	6362917830163629178301	30 TABLET, FILM COATED in 1 BOTTLE (63629-1783-1)Marketed from Jan 19, 2005
63629-1783-2	6362917830263629178302	60 TABLET, FILM COATED in 1 BOTTLE (63629-1783-2)Marketed from Jan 19, 2005
63629-1783-3	6362917830363629178303	20 TABLET, FILM COATED in 1 BOTTLE (63629-1783-3)Marketed from Jan 19, 2005
63629-1783-4	6362917830463629178304	21 TABLET, FILM COATED in 1 BOTTLE (63629-1783-4)Marketed from Jan 19, 2005
63629-1783-5	6362917830563629178305	90 TABLET, FILM COATED in 1 BOTTLE (63629-1783-5)Marketed from Jan 19, 2005
63629-1783-6	6362917830663629178306	120 TABLET, FILM COATED in 1 BOTTLE (63629-1783-6)Marketed from Jan 19, 2005
63629-1783-7	6362917830763629178307	28 TABLET, FILM COATED in 1 BOTTLE (63629-1783-7)Marketed from Jan 19, 2005

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Cimetidine
Generic name (nonproprietary): cimetidine
Active ingredients: Cimetidine — 300 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 63629
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074151
Marketing start: Nov 24, 2003
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 63629-1783_da171b05-5996-40eb-8258-1b4291a976acSPL ID da171b05-5996-40eb-8258-1b4291a976acSPL set ID 0ab5ea2b-bd2f-49ec-9e92-033bed998797RxCUI 197506UNII 80061L1WGD
Pharmacologic class: Histamine-2 Receptor Antagonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463629178301 followed by a unit qualifier and the quantity

Package 63629-1783-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 9, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Cimetidine tablets USP are indicated in: Short-term treatment of active duodenal ulcer. Most patients heal within 4 weeks and there is rarely reason to use cimetidine at full dosage for longer than 6 to 8 weeks (see DOSAGE AND ADMINISTRATION , Duodenal Ulcer ). Concomitant antacids should be given as needed for relief of pain. However, simultaneous administration of oral cimetidine and antacids is not recommended, since antacids have been reported to interfere with the absorption of oral cimetidine. Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of active ulcer. Patients have been maintained on continued treatment with cimetidine 400 mg …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63629-1783

What is NDC 63629-1783?: 63629-1783 is the product NDC for Cimetidine, Cimetidine 300 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cimetidine.
What is the active ingredient?: Cimetidine.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 63629. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cimetidine?: 21 other product NDCs are listed under this name. See all Cimetidine NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Cimetidine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-323	69452-0323-2069452-0323-30
Cimetidine	Cimetidine 300 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-324	69452-0324-2069452-0324-30
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-325	69452-0325-2069452-0325-30
Cimetidine	Cimetidine 800 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-326	69452-0326-2069452-0326-30
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-825	59651-0825-0159651-0825-05
Cimetidine	Cimetidine 800 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-826	59651-0826-01
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-697	51655-0697-51
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-0500	50090-0500-0050090-0500-01
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-333	63187-0333-30
Cimetidine	Cimetidine 800 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals USA, Inc.	0093-8305	00093-8305-01

All 22 Cimetidine NDCs

Other NDCs under ANDA 074151

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 074151
Product	Strength	Form · route	Labeler	Product NDC
Cimetidine	Cimetidine 300 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals USA, Inc.	0093-8192
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-0500
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-333